Congenital myasthenic syndrome 1A

MONDO:0011088

Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the CHRNA1 gene.

Also known as: CHRNA1 congenital myasthenic syndrome, CMS1A, congenital myasthenic syndrome caused by mutation in CHRNA1, congenital myasthenic syndrome type 1A, Cms IIa, Cms IIa, formerly, myasthenic syndrome, congenital, 1A, slow-channel, myasthenic syndrome, congenital, type IIa

0 clinical trials for this condition and its sub-types, 0 tagged with Congenital myasthenic syndrome 1A itself.

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↑ Postsynaptic congenital myasthenic syndrome (2)

Sub-types of Congenital myasthenic syndrome 1A

Myasthenic syndrome, congenital, 1B, fast-channel 0 trials

Including sub-types (0) Tagged with Congenital myasthenic syndrome 1A (0)

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